Ezquerra M - Search Results

1

A novel mutation (V89L) in the presenilin 1 gene in a family with early onset Alzheimer's disease and marked behavioural disturbances.

Queralt R, Ezquerra M, Lleó A, Castellví M, Gelpí J, Ferrer I, Acarín N, Pasarín L, Blesa R, Oliva R. Queralt R, et al. Among authors: ezquerra m. J Neurol Neurosurg Psychiatry. 2002 Feb;72(2):266-9. doi: 10.1136/jnnp.72.2.266. J Neurol Neurosurg Psychiatry. 2002. PMID: 11796781 Free PMC article.

2

Brain and Cerebrospinal Fluid α-Synuclein Real-Time Quaking-Induced Conversion Identifies Lewy Body Pathology in LRRK2-PD.

Garrido A, Fairfoul G, Tolosa E, Marti MJ, Ezquerra M, Green AJE. Garrido A, et al. Among authors: ezquerra m. Mov Disord. 2023 Feb;38(2):333-338. doi: 10.1002/mds.29284. Epub 2022 Dec 5. Mov Disord. 2023. PMID: 36471633

3

The genotype 2/2 of the presenilin-1 polymorphism is decreased in Spanish early-onset Alzheimer's disease.

Ezquerra M, Blesa R, Tolosa E, Lopez Pousa S, Aguilar M, Peña J, Van Broeckhoven C, Ballesta F, Oliva R. Ezquerra M, et al. Neurosci Lett. 1997 May 23;227(3):201-4. doi: 10.1016/s0304-3940(97)00328-5. Neurosci Lett. 1997. PMID: 9185685

4

Low apolipoprotein E epsilon4 allele frequency in the population of Catalonia (Spain) determined by PCR-RFLP and Laser fluorescent sequencer.

Gené M, Moreno P, Ezquerra M, Prat A, Huguet E, Adroer R, Oliva R. Gené M, et al. Among authors: ezquerra m. Eur J Epidemiol. 1997 Oct;13(7):841-3. doi: 10.1023/a:1007389303525. Eur J Epidemiol. 1997. PMID: 9384276

5

Alpha-antichymotrypsin gene polymorphism and risk for Alzheimer's disease in the Spanish population.

Ezquerra M, Blesa R, Tolosa E, Ballesta F, Oliva R. Ezquerra M, et al. Neurosci Lett. 1998 Jan 9;240(2):107-9. doi: 10.1016/s0304-3940(97)00924-5. Neurosci Lett. 1998. PMID: 9486483

6

Apolipoprotein E epsilon 4 alleles and meiotic origin of non-disjunction in Down syndrome children and in their corresponding fathers and mothers.

Ezquerra M, Ballesta F, Queralt R, Aledo R, Gómez D, Guitart M, Egozcue J, Ascaso C, Oliva R. Ezquerra M, et al. Neurosci Lett. 1998 May 22;248(1):1-4. doi: 10.1016/s0304-3940(98)00251-1. Neurosci Lett. 1998. PMID: 9665649

7

Significant changes in the tau A0 and A3 alleles in progressive supranuclear palsy and improved genotyping by silver detection.

Oliva R, Tolosa E, Ezquerra M, Molinuevo JL, Valldeoriola F, Burguera J, Calopa M, Villa M, Ballesta F. Oliva R, et al. Among authors: ezquerra m. Arch Neurol. 1998 Aug;55(8):1122-4. doi: 10.1001/archneur.55.8.1122. Arch Neurol. 1998. PMID: 9708963

8

Alpha1-antichymotrypsin gene polymorphism and susceptibility to Parkinson's disease.

Muñoz E, Obach V, Oliva R, Martí MJ, Ezquerra M, Pastor P, Ballesta F, Tolosa E. Muñoz E, et al. Among authors: ezquerra m. Neurology. 1999 Jan 15;52(2):297-301. doi: 10.1212/wnl.52.2.297. Neurology. 1999. PMID: 9932947

9

A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures.

Ezquerra M, Carnero C, Blesa R, Gelpí JL, Ballesta F, Oliva R. Ezquerra M, et al. Neurology. 1999 Feb;52(3):566-70. doi: 10.1212/wnl.52.3.566. Neurology. 1999. PMID: 10025789

10

Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.

Ballesta F, Queralt R, Gómez D, Solsona E, Guitart M, Ezquerra M, Moreno J, Oliva R. Ballesta F, et al. Among authors: ezquerra m. Ann Genet. 1999;42(1):11-5. Ann Genet. 1999. PMID: 10214502

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